Connect with us

Nigeria News

NAFDAC Approves Moderna And Sputnik COVID-19 Vaccines



United States: Expert Committee Recommends Pfizer Vaccine For 5-11 Year Olds

The National Agency for Food, Drug Administration and Control (NAFDAC) has approved the use of two more COVID-19 vaccines in Nigeria.

Naija News reports that the two vaccines approved are Moderna and the Sputnik vaccines.

NAFDAC approved both vaccines for emergency use in Nigeria to tackle COVID-19.

The Director-General of NAFDAC, Professor Moji Adeyeye, announced this on Thursday at a news conference in Abuja.

She explained that although the Sputnik vaccine has not yet been approved by the World Health Organisation, NAFDAC has carried out independent checks on the vaccine and found that the benefits outweigh the risks.

She disclosed that the agency has also approved the AstraZeneca vaccine from the Republic of Korea (SK Bioscience Co Limited).

This is as a result of the stall in the procurement of AstraZeneca vaccine, also known as Covishield, manufactured under licence by Serum Institute of India, due to the COVID-19 pandemic in the country.

Moderna is produced by Rovi Pharma Madrid, Spain while Sputnik V from Russia is by Gamaleya National Centre of Epidemiology and Microbiology.

NAFDAC is announcing the approval of Moderna and AstraZeneca vaccines and conditional approval of Sputnik V vaccine. The NAFDAC Vaccine Committee has been carefully assessing several vaccines despite the fact the vaccines have been approved by stringent regulatory countries or have received WHO’s Emergency Use Listing (EUL).

“A COVID-19 vaccine that has gone through the prior approval from either of these two sources had gone through quality, safety and efficacy evaluation which is a prerequisite for acceptance by COVAX Facility. Most regulatory agencies across the world use this mechanism to expedite their own regulatory approval to import and administer COVID-19 vaccines.

READ ALSO: NAFDAC cautions Nigerians against sanitisers with Methanol
“The agency spends at least 15 days to thoroughly examine the dossier or submission package of the vaccine to ensure that the benefits of the vaccine far outweigh the risks and any side effects are well noted for monitoring after vaccination by respective NAFDAC and Primary Health Officers.

“The EUL will allow Nigeria to receive supplies of the vaccines from the COVAX Facility. COVAX, the vaccines pillar of the Access to COVID-19 Tools (ACT) Accelerator Is jointly led by the Global Alliance for Vaccines and Immunisation (GAVI), the Coalition for Epidemic Preparedness Innovations (CEPI) and the World Health Organization (WHO).

“Its aim is to accelerate the development and manufacture of COVID-19 vaccines, and to guarantee fair and equitable access to low-middle income countries (LMIC) of which Nigeria is one.

“National Agency for Food and Drug Administration also gives full reviews for vaccines that have not gone through the EUL route. This mechanism is explained in our guidance developed by the COVID-19 Vaccine Committee.

“NAFDAC is the first National Regulatory Agency in Africa to have Guidance on Regulatory Preparedness for EUA, Licensing or Access to COVID-19 Vaccines,” she stated.